- Title
-
Short bowel syndrome results in increased gene expression associated with proliferation, inflammation, bile acid synthesis and immune system activation: RNA sequencing a zebrafish SBS model
- Authors
- Schall, K.A., Thornton, M.E., Isani, M., Holoyda, K.A., Hou, X., Lien, C.L., Grubbs, B.H., Grikscheit, T.C.
- Source
- Full text @ BMC Genomics
![]() ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions. PHENOTYPE:
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![]() ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions. |
![]() ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions. |
Increased β –catenin is detected by immunofluorescence in proximal SBS intestine compared to distal SBS and Sham intestine. Immunofluorescent detection of β –catenin identified more positive cells/hemivillus in SBS intestine compared to both the distal limb and sham proximal controls (A–C). Increased β –catenin is noted in the proximal SBS intestine (C; E) compared to distal SBS (D; E p = 0.001) and Sham proximal and SBS proximal intestine (A–C; E p = 0.012). No significant difference in β –catenin is seen between Sham proximal and distal intestine (A–B, E). A–D Scale 50 μm. (TIF 2151 kb) |